Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Lead diacetate trihydrate | HCID 22456 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 1,1-Dimethyl-3-(2-morpholinophenyl)thiourea | HCID 971192 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178457521 | HCID 178457521 | — |
Reaction Steps
A mixture of 1,1-dimethyl-3-(2-morpholinophenyl)thiourea (2.65 g prepared as described in Example 232), n-propylamine (1.6 ml), lead acetate trihydrate (3.8 g), potassium hydroxide (1.2 g) and ethanol (25 ml) was heated under reflux for 4 hours. A further amount of n-propylamine (1.6 ml) was added and the mixture heated under reflux for a further 8 hours. The reaction mixture yielded a residue which was extracted with ether. The extract was decolourised with charcoal, filtered and the solvent removed to leave a sticky solid which was dissolved in methanol (10 ml) and treated with fumaric acid to give 1,3-di-(n-propyl)-2-(2-morpholinophenyl)guanidine hemifumarate (m.p. 212°-214° C.) which was recrystallised from a 1:2 mixture of methanol and ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05223498 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-bec48f64d5ee40439715bb5535495988 |
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| Source note | uspto-grants-1993_06 |
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